A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155383



Internal ID22085888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16750987..16853833hg38UCSC Ensembl
Outerchr17:16749938..16860241hg38UCSC Ensembl
Innerchr17:16654301..16757147hg19UCSC Ensembl
Outerchr17:16653252..16763555hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38110304
hg19110304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010113
Samples
Known GenesCCDC144A, FAM106CP, KRT16P2, USP32P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155383
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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